Diisopropylethylamine → (S)-3-benzyloxycarbonylamino-1-[2-fluoro-5-(4-oxo-3,4-dihydrophthalazin-1-ylmethyl)phenyl]pyrrolidine-2,5-dione
反応式
C(N(C(C)C)CC)(C)C.[CH2:10]([O:17][C:18]([NH:20][C@H:21]([C:26]([NH:28][C:29]1[CH:34]=[C:33]([CH2:35][C:36]2[C:45]3[C:40](=[CH:41][CH:42]=[CH:43][CH:44]=3)[C:39](=[O:46])[NH:38][N:37]=2)[CH:32]=[CH:31][C:30]=1[F:47])=[O:27])[CH2:22][C:23]([OH:25])=O)=[O:19])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>CC(N(C)C)=O>[CH2:10]([O:17][C:18]([NH:20][C@H:21]1[CH2:22][C:23](=[O:25])[N:28]([C:29]2[CH:34]=[C:33]([CH2:35][C:36]3[C:45]4[C:40](=[CH:41][CH:42]=[CH:43][CH:44]=4)[C:39](=[O:46])[NH:38][N:37]=3)[CH:32]=[CH:31][C:30]=2[F:47])[C:26]1=[O:27])=[O:19])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1参加物
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
O-Benzotriazol-1-yl-N,N,N′N′-tetramethyluronium tetrafluoroborate (0.289 g, 0.9 mmol) and diisopropylethylamine (0.193 g, 1.5 mmol) were added sequentially to a stirred solution of (S)-3-benzyloxycarbonylamino-N-[2-fluoro-5-(4-oxo-3,4-dihydrophthalazin-1-ylmethyl)phenyl]succinamic acid (0.35 g, 0.68 mmol) in dimethylacetamide (3 ml), the mixture was stirred at ambient temperature for 24 hours, then it was added dropwise to stirred, ice-cold water (30 ml). The mixture was stirred for 1 hour, then the resulting solid was collected by filtration and dried in vacuo to give (S)-3-benzyloxycarbonylamino-1-[2-fluoro-5-(4-oxo-3,4-dihydrophthalazin-1-ylmethyl)phenyl]pyrrolidine-2,5-dione (0.238 g) as an off white solid, m.pt. 121–127° C. (softens 102° C.); m/z (M+H)+. 501, 96% purity.
後処理
- additionit was added dropwise
- stirringto stirred
- stirringThe mixture was stirred for 1 hour
- filtrationthe resulting solid was collected by filtration
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-aba67b767d724b3a8bd0dc51d0d26210
- 出典データセット
- uspto-grants-2007_03
- 特許番号
- US07196085B2
反応ノート
読み込み中…